A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1139087



Internal ID19264707
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:9709421..9709493hg38UCSC Ensembl
Outerchr3:9751105..9751177hg19UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg3873
hg1973
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3991711
SamplesKWS2
Known GenesCPNE9
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1139087
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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